BRIP1
protein-coding gene in the species Homo sapiens
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BRIP1
Summary
BRIP1 is a gene[1].
Key Facts
- BRIP1's instance of is recorded as gene[2].
- BRIP1 is a type of protein-coding gene[3].
- BRIP1's HomoloGene ID is recorded as 32766[4].
- BRIP1's genomic start is recorded as 59758627[5].
- BRIP1's genomic start is recorded as 61679139[6].
- BRIP1's genomic end is recorded as 59940882[7].
- BRIP1's genomic end is recorded as 61863559[8].
- BRIP1's ortholog is recorded as Brip1[9].
- BRIP1's ortholog is recorded as Brip1[10].
- BRIP1's ortholog is recorded as brip1[11].
- BRIP1's encodes is recorded as BRCA1 interacting protein C-terminal helicase 1[12].
- BRIP1's found in taxon is recorded as Homo sapiens[13].
- BRIP1's chromosome is recorded as human chromosome 17[14].
- BRIP1's genetic association is recorded as ovarian cancer[15].
- BRIP1's genetic association is recorded as Fanconi anemia complementation group J[16].
- BRIP1's genetic association is recorded as ovarian cancer[17].
- BRIP1's genetic association is recorded as breast carcinoma[18].
- BRIP1's strand orientation is recorded as reverse strand[19].
- BRIP1's exact match is recorded as http://identifiers.org/ncbigene/83990[20].
- BRIP1's cytogenetic location is recorded as 17q23.2[21].
- BRIP1's expressed in is recorded as ventricular zone[22].
- BRIP1's expressed in is recorded as gonad[23].
- BRIP1's expressed in is recorded as testicle[24].
- BRIP1's expressed in is recorded as secondary oocyte[25].
- BRIP1's expressed in is recorded as ganglionic eminence[26].